A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113252



Internal ID18909550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:13874016..13874075hg38UCSC Ensembl
Outerchr10:13916016..13916075hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3968159
SamplesKWS2
Known GenesFRMD4A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113252
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer